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Post Marketing Surveillance Study of Cuprimine

Scleroderma Clinical Trial

Official title:
Post Marketing Surveillance Study of Cuprimine (MK-0172-001)

Clinical Trial Summary

Cuprimine (penicillamine) was made available in the Philippines by the Sponsor under a Compassionate Special Permit issued by the Bureau of Food and Drugs. Physicians were able to request the drug for their patients from the Sponsor. A Clinical Study Report form was completed for each purchase of Cuprimine.

Clinical Trial Description

n/a

Study Design

N/A

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01374282
Study type Expanded Access
Source Merck Sharp & Dohme Corp.
Contact
Status No longer available
Phase N/A
View Details
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